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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400087Generated: November 2, 2026

Cesium carbonate → HCID 59233383, compound

https://huagongshe.com/reaction/1400087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant3-Bromo-4-methoxy-6-(trifluoromethyl)pyridazineHCID 59233382—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 59233383HCID 5923338363.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a stirred solution of 3-bromo-4-methoxy-6-trifluoromethyl-pyridazine (D6) (0.79 g, 3.07 mmol), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (0.74 g, 3.69 mmol) and cesium carbonate (2.0 g, 6.14 mmol) in toluene (15 ml) in a sealed tube under nitrogen, were added (R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.29 g, 0.46 mmol) and palladium(II) acetate (0.034 g, 0.15 mmol). The reactiom mixture was stirred at 110° C. for 18 h. After cooling to room temperature, the reaction mixture was filtered though Celite and the filtrate was evaporated. The crude product was purified by flash column chromatography (silica gel; 3% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. to yield D7 (0.73 g, 63%) as a yellow solid. C16H23F3N4O3 requires 376; Found 377 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906921B2
Source datasetuspto-grants-2014_12
ORD IDord-7df0ef6da96c4be39665fc50b5f4f2ba
Source noteuspto-grants-2014_12